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Peer Review reports

From: Carnitine palmitoyltransferase type 2 deficiency: novel mutation in a Native South American family with whole-body muscle magnetic resonance imaging findings: two case reports

Original Submission
7 Aug 2017 Submitted Original manuscript
19 Nov 2017 Reviewed Reviewer Report - Vijayakumar Javalkar
4 Apr 2018 Author responded Author comments - Daniela Avila
Resubmission - Version 2
4 Apr 2018 Submitted Manuscript version 2
Publishing
27 Apr 2018 Editorially accepted
28 Aug 2018 Article published 10.1186/s13256-018-1702-3

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Journal of Medical Case Reports

ISSN: 1752-1947